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Publication : Loss-of-function mutations in FREM2 disrupt eye morphogenesis.

First Author  Zhang X Year  2019
Journal  Exp Eye Res Volume  181
Pages  302-312 PubMed ID  30802441
Mgi Jnum  J:279933 Mgi Id  MGI:6368066
Doi  10.1016/j.exer.2019.02.013 Citation  Zhang X, et al. (2019) Loss-of-function mutations in FREM2 disrupt eye morphogenesis. Exp Eye Res 181:302-312
abstractText  Cryptophthalmos is a rare congenital disorder characterized by ocular dysplasia with eyelid malformation. Complete cryptophthalmos is characterized by the presence of continuous skin from the forehead over the eyes and onto the cheek, along with complete fusion of the eyelids. In the present study, we characterized the clinical manifestations of three patients with isolated bilateral cryptophthalmos. These patients shared the same c.6499C>T missense mutation in the FRAS1-related extracellular matrix protein 2 (FREM2) gene, while each individual presented an additional nonsense mutation in the same gene (Patient #1, c.2206C>T; Patient #2, c.5309G>A; and Patient #3, c.4063C>T). Then, we used CRISPR/Cas9 to generate mice carrying Frem2(R725X/R2156W) compound heterozygous mutations, and showed that these mice recapitulated the human isolated cryptophthalmos phenotype. We detected FREM2 expression in the outer plexiform layer of the retina for the first time in the cryptophthalmic eyes, and the levels were comparable to the wild-type mice. Moreover, a set of different expressed genes that may contribute secondarily to the phenotypes were identified by performing RNA sequencing (RNA-seq) of the fetal Frem2 mutant mice. Our findings extend the spectrum of FREM2 mutations, and provide insights into opportunities for the prenatal diagnosis of isolated cryptophthalmos. Furthermore, our work highlights the importance of the FREM2 protein during the development of eyelids and the anterior segment of the eyeballs, establishes a suitable animal model for studying epithelial reopening during eyelid development and serves as a valuable reference for further mechanistic studies of the pathogenesis of isolated cryptophthalmos.
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